Publication
| Jabs EW, Muller U, Li X, Ma L, Luo W, Haworth IS, Klisak I, Sparkes R, Warman ML, Mulliken JB, et al, A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis. Cell75:443-50 1993 |
| PubMed ID: 8106171 |
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| Records Return:
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| Catalog ID | Description | Collection_Type_id |
| MBP0002 | NIGMS HUMAN/RODENT SOMATIC CELL HYBRID MAPPING PANEL #2 DNA | |
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